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Katalyst CRO

Statistical Programmer

Katalyst CRO, New York

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  • The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
  • The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.
  • Develop and validate SAS programs to support clinical trial data analysis and reporting.
  • Create, maintain, and document SAS programming standards and procedures.
  • Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.
  • Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.
  • The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.
  • Prepare datasets for analysis, including merging and cleaning data from various sources.
  • Prepare and review tables, listings, and figures for clinical study reports.
  • Ensure compliance with regulatory requirements and guidelines.
  • Keep up to date with new SAS programming methods and software, as well as regulatory guidance.
Responsibilities
  • The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
  • The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.
  • Develop and validate SAS programs to support clinical trial data analysis and reporting.
  • Create, maintain, and document SAS programming standards and procedures.
  • Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.
  • Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.
  • The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.
  • Prepare datasets for analysis, including merging and cleaning data from various sources.
  • Prepare and review tables, listings, and figures for clinical study reports.
  • Ensure compliance with regulatory requirements and guidelines.
  • Keep up to date with new SAS programming methods and software, as well as regulatory guidance.
Requirements:
  • Bachelor's Degree in statistics, computer science, or a similar quantitative field.
  • 4+ years of clinical statistical programming experience within the pharmaceutical or related industry.
  • Proficiency in SAS programming.
  • Knowledge of CDISC data standards.
  • Strong attention to detail and ability to work independently.
  • Excellent problem-solving skills.
  • Excellent verbal and written communication skills.
  • Knowledge of regulatory requirements for clinical trials and drug development.
  • Ability to work in a team environment and collaborate effectively with other stakeholders.

Seniority level

  • Seniority level

    Associate

Employment type

  • Employment type

    Contract

Job function

  • Job function

    Information Technology

  • Industries

    Pharmaceutical Manufacturing

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